The goal of this pilot clinical trial is to assess a program of Home-based Adapted Physical Activity in Anorexia Nervosa.
The main questions it aims to answer are: Determining the acceptability of this program / Determining the feasibility and safety of this program / Determining patient satisfaction / Measuring the evolution of the symptomatology. Participants will follow a program of Home-based Adapted Physical Activity.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
36
There will be 8 weekly sessions at a time defined in advance for the same group and for the 8 sessions
Cécile BETRY
Grenoble, France
Pr GUILLAUME Sébastien
Montpellier, France
Acceptability of a telerehabilitation adapted physical activity (APA) program for patient with anorexia nervosa quantitatively
Number of patients who have realized the first of the 8 adapted physical activity session in relation to the total number of eligibly patients who have been invited to participate at the study
Time frame: at the first session of the APA program (Day 0)
Acceptability of a telerehabilitation adapted physical activity program for patient with anorexia nervosa qualitively
Reasons for refusal and participation's age will be collected anonymously for patients who refuse inclusion but agree to this informations being collected
Time frame: at the first session of the APA program (Day 0)
Feasibility and safety of a telerehabilitation adapted physical activity program for patients with anorexia nervosa quantitatively
Number and portion of patients who have realized the 8 adapted physical activity sessions as well as the first and final sessions
Time frame: at the end-of-study visit (Day 0 + 11 weeks)
Feasibility and safety of a telerehabilitation adapted physical activity program for patients with anorexia nervosa qualitively
Motifs of no realization of one ou more sessions will be collected. They will inclued technical problems, personal, professional ou medical constraints inclued study's exit for weight loss
Time frame: at the end-of-study visit (Day 0 + 11 weeks)
Patient satisfaction with the telerehabilitation adapted physical activity program for patients with anorexia nervosa quantitatively
Portion of patients answing "yes" at the question : "Would you like to continue this program ?"
Time frame: at the final session of APA programm (Day 0 + 8 weeks)
Patient satisfaction with the telerehabilitation adapted physical activity program for patients with anorexia nervosa qualitively
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Programm's motifs of satisfaction or no satisfaction will be collected during the final session of adapted physical activity program
Time frame: at the final session of APA programm (Day 0 + 8 weeks)
Measuring changes in symptomatology in key areas such as self-esteem through self-assessment questionnaire
Determination of this parameter :self-esteem by self-esteem scale of Rosenberg
Time frame: at the early study visit (Day 0 - 4 weeks) and at end-of-study visit (Day 0 + 11 weeks )
Measuring changes in symptomatology in key areas such as quality of life through self-assessment questionnaire
Determination of this parametes :quality of life by QUAVIAM scale
Time frame: at the early study visit (Day 0 - 4 weeks) and at end-of-study visit (Day 0 + 11 weeks )
Measuring changes in symptomatology in key areas such as dependence on physical activity through self-assessment questionnaire
Determination of this parameter : dependence on physical activity by EDQ questionnary
Time frame: at the early study visit (Day 0 - 4 weeks) and at end-of-study visit (Day 0 + 11 weeks )
Measuring changes in symptomatology in key areas such as dependence on physical activity through objective measure
Determination of this parameter : level of physical activity by 7-day actimetry recording
Time frame: at the early study visit (Day 0 - 4 weeks) and at end-of-study visit (Day 0 + 11 weeks )
Measuring changes in symptomatology in key areas such as changes in weight through objective measure
Determination of this parameter : weight in kilograms on a classic scale
Time frame: at the early study visit (Day 0 - 4 weeks) and at end-of-study visit (Day 0 + 11 weeks )
Measuring changes in symptomatology in key areas such as body composition through objective measure
Determination of this parameters : the body composition will be determinated by a impedancemetry measurement
Time frame: at the early study visit (Day 0 - 4 weeks) and at end-of-study visit (Day 0 + 11 weeks )